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FDA 510(k)

TABLE, X-RAY, RFX CLASSICAL

K-Number: K760466 · 1976-08-26

ApplicantGeneral Electric Co.
Decision Date1976-08-26
Product CodeIXR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TABLE, X-RAY, RFX CLASSICAL is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1976-08-26 under 510(k) number K760466. The device is classified under product code IXR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TABLE, X-RAY, RFX CLASSICAL?

TABLE, X-RAY, RFX CLASSICAL is a medical device that received FDA 510(k) clearance on 1976-08-26. The listed applicant is General Electric Co.. The 510(k) number is K760466.

When did TABLE, X-RAY, RFX CLASSICAL receive FDA 510(k) clearance?

TABLE, X-RAY, RFX CLASSICAL received FDA 510(k) clearance on 1976-08-26, under 510(k) number K760466.

Who is the listed applicant for TABLE, X-RAY, RFX CLASSICAL?

The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TABLE, X-RAY, RFX CLASSICAL?

The FDA product code for TABLE, X-RAY, RFX CLASSICAL is IXR.

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Related Devices (Code: IXR)

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K000412VISION R/F TILTING TABLEVilla Sistemi Medicali S.P.A.K973039LEGACY/LEGACY-D TABLEGE Medical SystemsK971128CAP-35B III/CINE 275Jamieson Film Co.K970640PHILIPS EASY DIAGNOSTPhilips Medical Systems North America, Inc.K965105ELECTROPHYSIOLOGY TILT TABLE MODEL #9660U.S. Imaging Tables, Inc.K965096FLUOROVIEW SERIES FLUOROSCOPIC TABLESU.S. Imaging Tables, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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